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Table 1 in Visualizing the spatial distribution of metabolites in Clausena lansium (Lour.) skeels using matrix-assisted laser desorption / ionization mass spectrometry imaging

Authors/Creators

  • 1. * & Institute of Quality Standard and Monitoring Technology for Agro-products of Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China & * & Key Laboratory of Testing and Evaluation for Agro-product Safety and Quality (Guangzhou), Ministry of Agriculture and Rural Affairs, China

Description

Table 1 Identification of metabolites in Clausena lansium (Lour.) Skeels by MALDI-MS analysis in positive ion mode.

Compound nameIon formulam/zFragment ionRef.
Alkaloids
DL-Stachydrine a[C H NO +K]+ 7 13 2182.06100.11
[C H N O –CO +H]+ 14 26 2 4 2243.21100.11, 144.10
[C H N O +K]+ 14 26 2 4325.15182.06, 144.10, 100.11
3-Methylcarbazole b[C H N H]+ 13 11 +182.1095.05, 167.07, 116.97, 105.05(Cui et al., 2002)
Murrayanine b[C H NO H]+ 14 11 2+226.09198.09,183.07,167.07,155.07(Sripisut et al., 2012)
Heptaphylline b[C H NO H]+ 17 17 +252.14234.13, 133.09, 91.05(Songsiang et al., 2011)
5-methyl-2-vinyl-3,11-dihydropyrano carbazole c[C H NO H]+ 18 15 +262.12205.10, 234.13, 91.05
Girinimbine a[C H NO + H]+ 18 17264.14131.05, 103.05, 205.10,
Murrastinine b[C H NO +H]+ 18 17 2280.13174.09, 205.10, 262.12(Liu et al., 2019)
Unknown[C H NO +K]+ 30 37 11626.20103.05, 131.05, 264.14, 500.16, 524.16
Unknown[C H NO K]+ 28 40 15+668.19103.05, 131.05, 264.14, 282.15
Coumarin
8-Hydroxylpsoralen[C H O H]+ 11 6 4+203.03147.04,175.04, 131.05(Huang et al., 2017)
Wampetin b[C H O H]+ 21 18 6+367.12203.03, 147.04, 131.05, 165.09(Liu et al., 2014)
2′,3′-Epoxyindicolactone b[C H O +H]+ 21 18 7383.11203.03, 163.08, 181.09(Lakshmi et al., 1984)
Anisolactone b[C H O +K]+ 21 18 6405.07–(Liu et al., 2014)
Dihydroindicolactone b[C H O K]+ 21 20 6+407.09203.03, 147.04, 167.11, 369.13(Liu et al., 2014)
Wampetin dimer c[C H O K]+ 42 36 12 +771.18405.07
Other metabolites
Sucrose[C H O K]+ 12 22 11+381.08219.03, 201.02
Hexose[C H O +K]+ 6 12 6219.03–
Citric acid[C H O +K]+ 6 8 7231.00–
4-Methylmethamphetamine[C H N + H]+ 11 17164.14–

a Confirmed by standard substance.

b The mass fragments used to infer the chemical identities of the various compounds are based on published literature provided for each of the alkaloids in the supplementary information.

c Hypothesis.

Notes

Published as part of Tang, Xuemei, Zhao, Meiyan, Chen, Zhiting, Huang, Jianxiang, Chen, Yan, Wang, Fuhua & Wan, Kai, 2021, Visualizing the spatial distribution of metabolites in Clausena lansium (Lour.) skeels using matrix-assisted laser desorption / ionization mass spectrometry imaging, pp. 4 in Phytochemistry (112930) 192 on page 4, DOI: 10.1016/j.phytochem.2021.112930, http://zenodo.org/record/8257146

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Identifiers

URL
http://table.plazi.org/id/24F50890A21E5409FFA8FF0E68A2FF63

Is cited by
Taxonomic treatment: 10.5281/zenodo.8269403 (DOI)
Taxonomic treatment: http://treatment.plazi.org/id/F823E90EA21F5409FFA8FC25690EF916 (URL)
Is part of
Journal article: 10.1016/j.phytochem.2021.112930 (DOI)
Journal article: urn:lsid:plazi.org:pub:041A9176A21D540AFFCCFF986B55FFA2 (LSID)
Journal article: http://publication.plazi.org/id/041A9176A21D540AFFCCFF986B55FFA2 (URL)
Journal article: http://zenodo.org/record/8257146 (URL)

References

  • Cui, C. B., Yan, S. Y., Cai, B., Yao, X. S., 2002. Carbazole alkaloids as new cell cycle inhibitor and apoptosis inducers from Clausena dunniana Levl. J. Asian Nat. Prod. Res. 4 (4), 233 - 241. https: // doi. org / 10.1080 / 1028602021000049041.
  • Sripisut, T., Cheenpracha, S., Ritthiwigrom, T., Prawat, U., Laphookhieo, S., 2012. Chemical constituents from the roots of Clausena excavata and their cytotoxicity. Record Nat. Prod. 6 (4), 386 - 389. https: // doi. org / 10.1017 / S 0009838800028895.
  • Songsiang, U., Thongthoom, T., Boonyarat, C., Yenjai, C., 2011. Claurailas A D, cytotoxic carbazole alkaloids from the roots ofClausena harmandiana. J. Nat. Prod. 74 (2), 208 - 212. https: // doi. org / 10.1021 / np 100654 m.
  • Liu, P. Y., Guo, J. M., Liu, Y. Y., Hu, S., Yan, G., Qiang, L., Fu, Y. H., 2019. Carbazole alkaloids with potential neuroprotective activities from the fruits of Clausena lansium. J. Agric. Food Chem. 67 (20), 5764 - 5771. https: // doi. org / 10.1021 / acs. jafc. 9 b 00961.
  • Huang, L., Feng, Z. L., Wang, Y. T., Lin, L. G., 2017. Anticancer carbazole alkaloids and coumarins from Clausena plants: a review. Chin. J. Nat. Med. 15 (12), 881 - 888. https: // doi. org / 10.1016 / S 1875 - 5364 (18) 30003 - 7.
  • Liu, H., Li, F., Li, C. J., Yang, J. Z., Li, L., Chen, N. H., Zhang, D. M., 2014. Bioactive furanocoumarins from stems of Clausena lansium. Phytochemistry (Oxf.) 107, 141 - 147. https: // doi. org / 10.1016 / j. phytochem. 2014.08. 002.
  • Lakshmi, V., Prakash, D., Raj, K., Kapil, R. S., Popli, S. P., 1984. Monoterpenoid furanocoumarin lactones from Clausena anisata. Phytochemistry 23 (11), 2629 - 2631. https: // doi. org / 10.1016 / S 0031 - 9422 (00) 84114 - X.